Variant report

Variant	rs59695980
Chromosome Location	chr13:97820229-97820230
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs16953899	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16953900	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17301278	0.96[EUR][1000 genomes]
rs2282424	0.91[EUR][1000 genomes]
rs4445760	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4456365	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57348783	0.94[EUR][1000 genomes]
rs57806253	0.94[EUR][1000 genomes]
rs61107763	0.91[EUR][1000 genomes]
rs7317886	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7317904	0.94[EUR][1000 genomes]
rs7322677	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7322973	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7331281	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7332127	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7332327	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7337250	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7338056	0.94[EUR][1000 genomes]
rs7338420	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7338629	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7983632	0.86[EUR][1000 genomes]
rs7983895	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7988998	0.94[EUR][1000 genomes]
rs7989356	0.91[EUR][1000 genomes]
rs7990235	0.94[EUR][1000 genomes]
rs7990802	0.84[EUR][1000 genomes]
rs7995449	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7997574	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9513209	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9513210	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9513211	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9513214	0.96[EUR][1000 genomes]
rs9513215	0.94[EUR][1000 genomes]
rs9513216	0.96[EUR][1000 genomes]
rs9516832	0.90[EUR][1000 genomes]
rs9516834	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9516835	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9516840	0.85[ASN][1000 genomes]
rs9516841	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9516843	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9516844	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9516845	0.94[EUR][1000 genomes]
rs9516846	0.94[EUR][1000 genomes]
rs9516847	0.94[EUR][1000 genomes]
rs9516848	0.94[EUR][1000 genomes]
rs9516849	0.94[EUR][1000 genomes]
rs9516850	0.94[EUR][1000 genomes]
rs9516853	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1137	chr13:97803474-97848814	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:97816200-97824200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:97816200-97830600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:97820200-97820600	Enhancers	Gastric	stomach
4	chr13:97820200-97821000	Enhancers	Stomach Mucosa	stomach

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